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Synthesis and spectroscopic properties of beta-meso directly linked porphyrin-corrole hybrid compounds

Temelli, Baris; Kalkan, Hilal


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  <dc:creator>Temelli, Baris</dc:creator>
  <dc:creator>Kalkan, Hilal</dc:creator>
  <dc:date>2018-01-01</dc:date>
  <dc:description>The preparation of beta-meso directly linked porphyrin-corrole hybrids was realized for the first time via an InCl3-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by H-1 NMR, C-13 NMR, 2D NMR, UV-vis absorption and fluorescence spectroscopy.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/30911</dc:identifier>
  <dc:identifier>oai:zenodo.org:30911</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 14 187-193</dc:source>
  <dc:title>Synthesis and spectroscopic properties of beta-meso directly linked porphyrin-corrole hybrid compounds</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
</oai_dc:dc>
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